About the Role
A leading biotechnology firm in Toronto is seeking a GMP Manufacturing Specialist to develop and execute cGMP manufacturing processes for cell therapeutics in clinical trials. The role involves handling raw materials, writing SOPs, and ensuring compliance with stringent guidelines. Candidates should have a BS in a relevant field and experience in aseptic techniques. This contract position offers an opportunity to work on the forefront of gene therapy production within a dynamic and fast-paced environment.
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